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All the main constructs included in the analysis were assessed with self-report measures based on multi-item scales.
Stationarity and convergence of the Bayesian analysis were assessed with Tracer v1.5 [ 102].
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To estimate errors of GFRFDG and ERPFFDG, the reproducibility of the VOI choice for FDG TAC analysis was assessed with data from subject group 1 (Table 1), having high differences between their reference values, age, and gender.
Nodal support within the phylogenetic trees within the parsimony analysis was assessed with bootstrap percentage after 1000 re-sampling steps [45] and within the maximum likelihood analysis with jackknife percentage after 1000 re-sampling steps with 30% character deletion [46].
The trend analysis was assessed with Cochran-Armitage trend test.
Statistical analysis was assessed with the Analyst Interface of the SAS Statistical Analysis Systemm) Version 9.2.
Statistical significance for global analysis was assessed with a false discovery rate (FDR) of 1%, q-value ≤0.01.
Gene ontology enrichment analysis was assessed with the hypergeometric statistic as implemented in the R-package GOstats [ 20] (Version: 2.32.0), with all genes on the microarray as background.
For the primary outcome (filter lifespan), survival analysis was assessed with Kaplan-Meier curves and groups were compared by log rank test.
The adequacy of the factor analysis was assessed with the Kaiser-Meyer-Olkin measure and the Bartlett's test of sphericity [ 15].
PCA and phylogenetic analysis provided very similar patterns of association when the Australian nest groups of L. humile identified by Bayesian analysis were assessed together with the 11 potential source populations (Fig. 4).
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